Clinical Trials Training
VST Research offers a wide range of courses to our customers including technical aspects such as monitoring, data-management, medical writing, pharmacovigilance, audits and inspections and also regulatory requirements and guidelines such as national legislation, the Declaration of Helsinki, GCP and other ICH guidelines, plus EU-Directives. These trainings can be held in any location in order to meet individual companies’ training requirements.
Our training courses include:
- Application to Ethics committees
- Audits and Inspections
- Biostatistics for non-statisticians
- Biostatistics, Advanced
- Clinical Study Protocol Writing
- Clinical trials in the pediatric population
- Contracts and Agreements
- Effective Site Management
- EU directives
- Good Clinical Practice
- GCP update
- Introduction to Clinical Research
- Medical and Scientific Writing
- Medical Devices
- Monitoring, Basic
- Monitoring Advanced
- Non-Interventional studies
- Patient Information
- Pharmacovigilance
- Presentation skills
- Project Management for Clinical Research
- Regulatory Affairs
